Treating Post-Operative Thirst With Flavoured Ice Lollies or Water - a Comparative Study to Improve Post-operative Discomfort
THIRST
1 other identifier
interventional
173
1 country
1
Brief Summary
Patients are asked not to eat and drink before their operation, and the investigators know that this can make people feel thirstier when they wake up from their anaesthetic. The investigators want to know if giving patients ice lollies improves their thirst more than if they were given water. Gloucestershire Royal Hospital is funding and running a research study to find ways to try and improve this.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 19, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 17, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
May 17, 2021
CompletedFirst Submitted
Initial submission to the registry
August 21, 2023
CompletedFirst Posted
Study publicly available on registry
August 28, 2023
CompletedMarch 12, 2026
March 1, 2026
28 days
August 21, 2023
March 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The primary outcome measure is the level of post-operative thirst following intervention with either water or ice lolly.
Data on pre and post-intervention thirst will be recorded using questionnaires and a numerical rating score from 0 to 10, with 0 being no thirst at all and 10 being very thirsty. These scores will also be sub-divided into no thirst (0), mild thirst (1-3), moderate thirst (4-7) and severe thirst (8-10). This data will undergo statistical analysis to challenge the null hypothesis for the primary outcome measure.
Intervention is to be given when the patient is adequately recovered from anaesthesia. An initial thirst score is recorded, then intervention given. Thirst scores are recorded again 15 minutes later to provide data for the primary outcome measure.
Study Arms (2)
Patients allocated ice lollies to treat post-operative thirst
EXPERIMENTALIce lollies consisted of a flavoured ice popsicle (blackcurrant) provided through hospital catering. Participants were allocated a single ice popsicle with thirst scores recored pre and post intervention.
Patients allocated water as control comparison
OTHERWater is a routine treatment for post-operative thirst and therefore used a control to compare our intervention against.
Interventions
Blackcurrant flavoured ice popsicles, 105ml volume.
Water from tap, one cup given by recovery nurses.
Eligibility Criteria
You may qualify if:
- Patients over 18 years of age
- Patients attending for elective surgery
You may not qualify if:
- Allergy to products within the ice lolly
- Designated nil-by-mouth by anaesthetic or surgical teams
- Patient less than 18 years old
- Patient unable to give consent
- Refusal of patient to be involved with study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Gloucestershire Royal Hospital
Gloucester, Gloucestershire, GL1 3NN, United Kingdom
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
David Sleep, BSc MSc MBBS D.Phil
Gloucestershire Hospitals NHS Foundation Trust
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 21, 2023
First Posted
August 28, 2023
Study Start
April 19, 2021
Primary Completion
May 17, 2021
Study Completion
May 17, 2021
Last Updated
March 12, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
This is a small centre study with a minor intervention. Participant information is limited to demographic and operative data only.